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Reference Laboratory
Tests 		 
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Antimicrobial Susceptibility, AFB print

In order to perform susceptibility testing and to interpret test results, the identification of the isolate is required.

51200 - AFB Susceptibility, Custom Drug Panel (1)
51205 - AFB Susceptibility, Custom Drug Panel (2)
51210 - AFB Susceptibility, Custom Drug Panel (3)


Please see the following technical sheet for more information:
 Antimicrobial Testing
Methodology
Reference Range By report
Preferred Specimen Pure culture safely contained.
Transport Temperature 2-28° C
Results Available 14 to 21 days
CPT Code 87190 per Drug
 
81175
Adenovirus Serotyping
-240
Typhus Fever (See Rickettsia [Typhus Fever Group])
-241
U1 snRNP (See RNP Antibody)
-242
Vaccine Response Assays (See assays: Bordetella pertussis, Diphtheria, Haemophilus, Meningococcal, Polio Neutralization, Pneumococcal, or Tetanus, or panels: Humoral Immunity Evaluation, Immune Status Panel or Tetanus/Diphtheria Panel).
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-243
Valley Fever (See Coccidioides)
-244
Vancomycin-Resistant Enterococcus
(See Bacterial Culture, Screen for Vancomycin-Resistant Enterococcus)
-245
Vibrio cholera Culture (See Bacterial Culture, Aerobic, Stool)
-246
Viral Culture, Rapid (See Herpes Simplex Virus Rapid Culture, Cytomegalovirus Rapid Culture,
Influenza Virus Rapid Culture, Respiratory Virus Rapid Culture,
or Varicella-Zoster Virus Rapid Culture)
-247
Viral Serum Level (See Antiviral Serum Level)
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-248
Viral Susceptibility Testing (See Antiviral Susceptibility)
 
First FDA Clearance of a 2009 H1N1 Test Given to Focus Diagnostics


FDA Issues Another Emergency Use Authorization for Commercial H1N1 Flu Test to Quest Diagnostics’ Focus Diagnostics


Focus Diagnostics provides the first commercial test for detecting the 2009 H1N1 influenza virus that the FDA has authorized for emergency use.


Focus Diagnostics receives NYSDOH exemption for Diagnostic Immunology and Serology testing services


Focus Diagnostics Launches Laboratory Test for Chikungunya Virus


 
   
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